Package 70771-1597-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70771-1597-1
Digits Only 7077115971
Product NDC 70771-1597
Product ID 70771-1597_027de750-bb64-4f6c-87ee-9c73862af579
Description

100 TABLET in 1 BOTTLE (70771-1597-1)

Marketing

Marketing Status
Marketed Since 2020-09-17
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Midodrine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "027de750-bb64-4f6c-87ee-9c73862af579", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["b4c4417e-d8fd-46c8-b82f-ffbc8f201752"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1597-1)", "package_ndc": "70771-1597-1", "marketing_start_date": "20200917"}], "brand_name": "Midodrine hydrochloride", "product_id": "70771-1597_027de750-bb64-4f6c-87ee-9c73862af579", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "70771-1597", "generic_name": "Midodrine hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213055", "marketing_category": "ANDA", "marketing_start_date": "20200917", "listing_expiration_date": "20261231"}